Vital roles of mTOR complex 2 in Notch-driven thymocyte differentiation and leukemia

Keunwook Lee, Ki Taek Nam, Sung Hoon Cho, Prathyusha Gudapati, Yoonha Hwang, Do Sim Park, Ross Potter, Jin Chen, Emmanuel Volanakis, Mark Boothby

Research output: Contribution to journalArticlepeer-review

94 Citations (Scopus)


Notch plays critical roles in both cell fate decisions and tumorigenesis. Notch receptor engagement initiates signaling cascades that include a phosphatidylinositol 3-kinase/target of rapamycin (TOR) pathway. Mammalian TOR (mTOR) participates in two distinct biochemical complexes, mTORC1 and mTORC2, and the relationship between mTORC2 and physiological outcomes dependent on Notch signaling is unknown. In this study, we report contributions of mTORC2 to thymic T-cell acute lymphoblastic leukemia (T-ALL) driven by Notch. Conditional deletion of Rictor, an essential component of mTORC2, impaired Notch-driven proliferation and differentiation of pre-T cells. Furthermore, NF-κB activity depended on the integrity of mTORC2 in thymocytes. Active Akt restored NF-κB activation, a normal rate of proliferation, and differentiation of Rictor-deficient pre-T cells. Strikingly, mTORC2 depletion lowered CCR7 expression in thymocytes and leukemic cells, accompanied by decreased tissue invasion and delayed mortality in T-ALL driven by Notch. Collectively, these findings reveal roles for mTORC2 in promoting thymic T cell development and T-ALL and indicate that mTORC2 is crucial for Notch signaling to regulate Akt and NF-κB.

Original languageEnglish
Pages (from-to)713-728
Number of pages16
JournalJournal of Experimental Medicine
Issue number4
Publication statusPublished - 2012 Apr 9

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology


Dive into the research topics of 'Vital roles of mTOR complex 2 in Notch-driven thymocyte differentiation and leukemia'. Together they form a unique fingerprint.

Cite this